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Mectron

FDA UDI

Class II (US FDA UDI)

by Mectron Spa

Identity

Trade Name
MECTRON FDA UDI
Generic Name
Dental ultrasonic surgical system handpiece tip FDA UDI
Device Name
PP1 is a dental insert for root surface micro-smoothering to be used in conjunction with Mectron Piezosurgery ultrasonic handpieces. FDA UDI
Model / Reference
PP1 FDA UDI
Description
PP1 is a dental insert for root surface micro-smoothering to be used in conjunction with Mectron Piezosurgery ultrasonic handpieces. FDA UDI

Identifiers

Catalog Number
03180002 FDA UDI
Primary DI / UDI-DI
E322031800020 FDA UDI
510(k) Number
K151248 FDA UDI
FDA Product Code
ELC FDA UDI
DZI FDA UDI
GMDN Term
Dental ultrasonic surgical system handpiece tip FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.4850 FDA UDI
872.4120 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Dental ultrasonic surgical system handpiece tip

Mectron by Mectron Spa — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental ultrasonic surgical system handpiece tip.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Mectron Spa

Sources (1)

  • FDA UDI 9bfa0597-6d3b-4b9e-b02b-33f0d2557ef6 36 fields · synced May 30, 2026